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1.
JAMA Netw Open ; 7(6): e2415220, 2024 Jun 03.
Article in English | MEDLINE | ID: mdl-38842808

ABSTRACT

Importance: People with HIV (PWH) may be at increased risk for severe outcomes with COVID-19 illness compared with people without HIV. Little is known about COVID-19 vaccination coverage and factors associated with primary series completion among PWH. Objectives: To evaluate COVID-19 vaccination coverage among PWH and examine sociodemographic, clinical, and community-level factors associated with completion of the primary series and an additional primary dose. Design, Setting, and Participants: This retrospective cohort study used electronic health record data to assess COVID-19 vaccination information from December 14, 2020, through April 30, 2022, from 8 health care organizations of the Vaccine Safety Datalink project in the US. Participants were adults diagnosed with HIV on or before December 14, 2020, enrolled in a participating site. Main Outcomes and Measures: The percentage of PWH with at least 1 dose of COVID-19 vaccine and PWH who completed the COVID-19 vaccine primary series by December 31, 2021, and an additional primary dose by April 30, 2022. Rate ratios (RR) and 95% CIs were estimated using Poisson regression models for factors associated with completing the COVID-19 vaccine primary series and receiving an additional primary dose. Results: Among 22 058 adult PWH (mean [SD] age, 52.1 [13.3] years; 88.8% male), 90.5% completed the primary series by December 31, 2021. Among 18 374 eligible PWH who completed the primary series by August 12, 2021, 15 982 (87.0%) received an additional primary dose, and 4318 (23.5%) received a booster dose by April 30, 2022. Receipt of influenza vaccines in the last 2 years was associated with completion of the primary series (RR, 1.17; 95% CI, 1.15-1.20) and an additional primary dose (RR, 1.61; 95% CI, 1.54-1.69). PWH with uncontrolled viremia (HIV viral load ≥200 copies/mL) (eg, RR, 0.90 [95% CI, 0.85-0.95] for viral load 200-10 000 copies/mL vs undetected or <200 copies/mL for completing the primary series) and Medicaid insurance (eg, RR, 0.89 [95% CI, 0.87-0.90] for completing the primary series) were less likely to be fully vaccinated. By contrast, greater outpatient utilization (eg, RR, 1.07 [95% CI, 1.05-1.09] for ≥7 vs 0 visits for primary series completion) and residence in counties with higher COVID-19 vaccine coverage (eg, RR, 1.06 [95% CI, 1.03-1.08] for fourth vs first quartiles for primary series completion) were associated with primary series and additional dose completion (RRs ranging from 1.01 to 1.21). Conclusions and Relevance: Findings from this cohort study suggest that, while COVID-19 vaccination coverage was high among PWH, outreach efforts should focus on those who did not complete vaccine series and those who have uncontrolled viremia.


Subject(s)
COVID-19 Vaccines , COVID-19 , HIV Infections , SARS-CoV-2 , Vaccination Coverage , Humans , Male , Female , Middle Aged , COVID-19/prevention & control , Retrospective Studies , Vaccination Coverage/statistics & numerical data , Adult , COVID-19 Vaccines/administration & dosage , United States , Aged , Vaccination/statistics & numerical data
2.
Emerg Infect Dis ; 29(9): 1855-1858, 2023 09.
Article in English | MEDLINE | ID: mdl-37437558

ABSTRACT

We report 2 cases of pharyngeal monkeypox virus and group A Streptococcus co-infection in the United States. No rash was observed when pharyngitis symptoms began. One patient required intubation before mpox was diagnosed. Healthcare providers should be aware of oropharyngeal mpox manifestations and possible co-infections; early treatment might prevent serious complications.


Subject(s)
Coinfection , Mpox (monkeypox) , Streptococcal Infections , Humans , United States/epidemiology , Monkeypox virus , Streptococcus pyogenes , Pharynx , Streptococcal Infections/diagnosis , Streptococcal Infections/epidemiology
3.
Am J Trop Med Hyg ; 95(5): 1161-1165, 2016 Nov 02.
Article in English | MEDLINE | ID: mdl-27807296

ABSTRACT

Zika virus (ZIKV) is a mosquito-borne flavivirus with a significant public health impact highlighted by the ongoing epidemic in the Americas. We describe a 44-year-old male presenting to our tropical medicine center with complaints of fever, headache, joint pain, and rash after recent travel to Guyana. The patient subsequently developed gait imbalance and lower extremity weakness with clinical examination, cerebrospinal fluid studies, and magnetic resonance imaging of the spine consistent with a diagnosis of Guillain-Barré syndrome (GBS). ZIKV infection was confirmed via detection of ZIKV RNA in urine by polymerase chain reaction. The patient was treated with intravenous immunoglobulin and experienced near-complete neurologic recovery, reporting ongoing mild paresthesia up to 2 months later. This case highlights the diagnostic challenges posed by ZIKV and underscores the need for clinician awareness of the potential for neurological complications such as GBS with ZIKV infection.


Subject(s)
Guillain-Barre Syndrome/diagnosis , Zika Virus Infection/diagnosis , Adult , Epidemics , Guillain-Barre Syndrome/complications , Guillain-Barre Syndrome/drug therapy , Guyana , Humans , Immunoglobulins, Intravenous/therapeutic use , Magnetic Resonance Imaging , Male , RNA, Viral/isolation & purification , Travel , Zika Virus , Zika Virus Infection/complications
4.
Diagn Microbiol Infect Dis ; 76(3): 356-60, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23659829

ABSTRACT

We report the prevalence of carbapenemase-positive Klebsiella pneumoniae among clinical isolates collected from US medical centers (n = 42) from 2007-2009 through the SENTRY Antimicrobial Surveillance Program. Isolates with imipenem or meropenem MIC ≥ 2 µg/mL were screened by PCR for various carbapenemase genes. Of 2049 K. pneumoniae isolates, 126 (6.1%) were non-susceptible to imipenem or meropenem. blaKPC was identified in 113 isolates (5.5%). No other carbapenemase genes were identified. For US regions combined, prevalence of K. pneumoniae carbapenemase (KPC)-positive isolates were 5.9% in 2007, 4.9% in 2008, and 5.7% in 2009. Rates were highest in the Mid-Atlantic region (28.6% overall), with fluctuation over time (29%, 23%, and 33% from 2007-2009), followed by the East North Central region (2.4% overall), with a slightly increasing trend (nil, 3.1%, 3.8% from 2007-2009). All KPC-positive organisms were carbapenem non-susceptible according to updated CLSI breakpoints, although all but one was similarly classified according to previous breakpoints.


Subject(s)
Bacterial Proteins/genetics , Klebsiella Infections/epidemiology , Klebsiella pneumoniae/enzymology , beta-Lactam Resistance/genetics , beta-Lactamases/genetics , Antineoplastic Agents/pharmacology , Carbapenems/pharmacology , Epidemiological Monitoring , Hospitals , Humans , Klebsiella Infections/microbiology , Klebsiella pneumoniae/genetics , Microbial Sensitivity Tests , Prevalence , United States/epidemiology
5.
J Infect Dis ; 191(1): 33-9, 2005 Jan 01.
Article in English | MEDLINE | ID: mdl-15593000

ABSTRACT

In 2000, a large international outbreak of meningococcal disease caused by Neisseria meningitidis serogroup W-135 was identified among pilgrims returning from the Hajj in Saudi Arabia. To assess ongoing risk, we evaluated N. meningitidis carriage among US travelers to the 2001 Hajj. Of 25 N. meningitidis isolates obtained, 15 (60%) were nongroupable and 8 (32%) were serogroup W-135 when tested by standard slide-agglutination techniques. Two additional nongroupable isolates were characterized as serogroup W-135 when tested by polymerase chain reaction. Nine of 10 serogroup W-135 isolates were indistinguishable from the Hajj-2000 clone. None of the departing, but 9 (1.3%) of the returning, pilgrims carried serogroup W-135 (P=.01); all carriers reported previous vaccination. Carriage of N. meningitidis serogroup W-135 increased significantly in pilgrims returning from the Hajj. Although the risk of disease to pilgrims appears to be low, the risk of spread to others of this pathogenic strain remains a concern.


Subject(s)
Carrier State/epidemiology , Meningococcal Infections/epidemiology , Neisseria meningitidis, Serogroup W-135/isolation & purification , Travel , Adult , Aged , Carrier State/microbiology , Female , Humans , Islam , Male , Meningococcal Infections/microbiology , Middle Aged , Neisseria meningitidis, Serogroup W-135/classification , Pharynx/microbiology , Polymerase Chain Reaction , Saudi Arabia , Serotyping , United States
6.
Clin Infect Dis ; 38(6): 799-804, 2004 Mar 15.
Article in English | MEDLINE | ID: mdl-14999621

ABSTRACT

Bordetella holmesii is a recently identified gram-negative bacterial species associated with bacteremia, endocarditis, and respiratory illness, mainly in immunocompromised patients. From isolates submitted to the Centers for Disease Control and Prevention from 1983 through 2000 for further identification, we identified 30 patients with B. holmesii bacteremia. Of the 26 patients for whom data were available, 22 (85%) were anatomically or functionally asplenic. In 25 (96%) of the 26 patients, B. holmesii was the only organism isolated from blood samples, and 14 patients (54%) had B. holmesii recovered from > or =2 blood cultures. The clinical course of the infection was generally characterized by a nonspecific febrile illness. Twenty-one patients (81%) were treated with various antimicrobial agents, and 20 (77%) were admitted to the hospital. There were no deaths. Our findings support evidence that B. holmesii may be a true pathogen associated with bacteremia among asplenic patients.


Subject(s)
Bacteremia/microbiology , Bordetella Infections/microbiology , Bordetella/isolation & purification , Adolescent , Adult , Aged , Aged, 80 and over , Bacteremia/drug therapy , Bordetella/genetics , Bordetella Infections/drug therapy , Child , Child, Preschool , Female , Humans , Infant , Male , Middle Aged , RNA, Ribosomal, 16S/analysis , Treatment Outcome
7.
Emerg Infect Dis ; 9(5): 515-9, 2003 May.
Article in English | MEDLINE | ID: mdl-12737732

ABSTRACT

We examined outbreak investigations conducted around the world from 1988 to 1999 by the Centers for Disease Control and Prevention's Epidemic Intelligence Service. In 44 (4.0%) of 1,099 investigations, identified causative agents had bioterrorism potential. In six investigations, intentional use of infectious agents was considered. Healthcare providers reported 270 (24.6%) outbreaks and infection control practitioners reported 129 (11.7%); together they reported 399 (36.3%) of the outbreaks. Health departments reported 335 (30.5%) outbreaks. For six outbreaks in which bioterrorism or intentional contamination was possible, reporting was delayed for up to 26 days. We confirmed that the most critical component for bioterrorism outbreak detection and reporting is the frontline healthcare profession and the local health departments. Bioterrorism preparedness should emphasize education and support of this frontline as well as methods to shorten the time between outbreak and reporting.


Subject(s)
Bioterrorism/prevention & control , Communicable Disease Control , Disaster Planning/organization & administration , Disease Outbreaks/prevention & control , Population Surveillance , Centers for Disease Control and Prevention, U.S. , Communicable Diseases/diagnosis , Communicable Diseases/epidemiology , Humans , United States
8.
Emerg Infect Dis ; 8(2): 171-4, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11897069

ABSTRACT

From 1974 to 1998, 22 isolates of an unusual bacterium, designated as CDC nonoxidizer 1 group (NO-1), were sent to the Centers for Disease Control and Prevention for identification. The organism's phenotypic characteristics were similar to asaccharolytic strains of Acinetobacter, but differed in their cellular morphology and cellular fatty acid profile. We report here on NO-1's clinical and epidemiologic significance. In all cases, isolates were recovered from an animal bite wound; 17 (77%) were isolated from a dog bite wound, 4 (18%) from a cat bite wound, and one (5%) from an unspecified animal bite. Clinical data were retrieved and reviewed for 12 (55%) of the 22 bite victims. None of the patients had pre-existing conditions associated with immunosuppression. Seven (58%) patients were hospitalized for a median stay of 4 days (range, 2 to 11 days). The median time between bite to the worsening of symptoms was 17.5 hours (range, 3 to 78 hours). All patients recovered following antibiotic treatment.


Subject(s)
Acinetobacter Infections/epidemiology , Acinetobacter Infections/microbiology , Acinetobacter/isolation & purification , Bites and Stings/epidemiology , Bites and Stings/microbiology , Adolescent , Adult , Aged , Animals , Bacterial Typing Techniques , Cats , Centers for Disease Control and Prevention, U.S. , Child , Child, Preschool , Dogs , Female , Humans , Infant , Male , Middle Aged , United States/epidemiology
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